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NCT Number: NCT06059872

Biomarkers of Reaction To HIIT Exercise

Stroke survivors with lower limb disability can improve their walking speed with high-intensity interval training (HIIT) rehabilitation therapy. However, some individuals may not respond to HIIT even when fully adherent to the program. To address this, the investigators propose to build a predictive model that identifies if a Veteran with chronic subcortical stroke will improve their walking speed with HIIT by incorporating blood lactate as an early predictor of exercise response, and inhibitory neurotransmitter gamma-aminobutyric acid (GABA) and regional cerebral blood flow (CBF) as predictors of the brain's potential to respond, while also taking into consideration other factors such as comorbidities, demographics, and fitness levels.

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Key information

Age range

18 year–89 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Atlanta VA Medical and Rehab Center, Decatur, GA

Decatur, Georgia, 30033-4004, United States

Location status: Recruiting

Location contact

Lisa C Krishnamurthy, PhD

CONTACT

[email protected]

404-321-6111 ext. 6235

Lisa C Krishnamurthy, PhD

PRINCIPAL_INVESTIGATOR

About this study

Most chronic subcortical stroke survivors have difficulty walking, but few predictors can help identify if a patient will respond to an exercise regimen and improve their function. To enhance precision rehabilitation for chronic subcortical stroke patients, personalized aerobic exercise interventions are crucial. This requires the development of innovative technologies that can identify the essential neurobiological factors to predict intervention response and enable clinicians to determine individualized rehabilitation targets. Lactate is one exciting new target that acts as a molecular messenger between the periphery and the brain. For lactate to have an impact on other organs, including the brain, there must be a substantial increase in its level in the bloodstream from baseline. When the blood lactate threshold is surpassed during exercise, lactate acts on the brain metabolically via the TCA cycle. Embedded within the TCA cycle is the means to increase or decrease neurotransmitter concentrations such as GABA and glutamate. Gamma-aminobutyric acid (GABA), the brain's major inhibitory neurotransmitter, is a new treatment target that promotes neural plasticity during stroke rehabilitation. Drawing from the framework of personalized rehabilitation approaches and our preliminary data, the investigators propose to build a predictive model that can identify if a chronic subcortical stroke patient will respond to exercise training. This model aims to predict improvements in walking speed by incorporating blood lactate as an early predictor of exercise response and GABA and cerebral blood flow (CBF) as predictors of the brain's potential to respond, in addition to other influencing factors such as comorbidities, demographics, and fitness levels. The overarching hypothesis is that robust neurophysiological factors driven by lactate can differentiate responders from resistors and that these factors can be applied clinically as biomarkers to predict functional outcomes after a 12-week HIIT intervention. The investigators will assess improvements in walking speed in 48 Veterans with lower limb disability due to chronic subcortical stroke in response to a 36-session (12-week) HIIT intervention. After the intervention, each adherent participant who improves their walking speed to greater than 0.6 m/s will be categorized as a responder while each adherent participant who does not improve their walking speed will be categorized as a resistor. At baseline and after 12 weeks of HIIT the investigators will evaluate walking speed, balance, leg strength, and endurance to identify resistors and responders to HIIT and collect a) GABA from the primary sensory-motor leg area using single-voxel magnetic resonance spectroscopy, b) CBF from the whole brain using pseudo-Continuous Arterial Spin Labeling MRI and c) VO2 max to evaluate change in CRF. During the intervention, the investigators will collect blood lactate via finger prick during sessions 1, 4, 7, 10, and 28 to assess its potential as an early predictor of exercise response. In aim 1 the investigators determine if surpassing the lactate threshold during the first 4 weeks of HIIT predicts the change in walking speed to 0.6 m/s, from pre- to post-HIIT. If lactate proves to be a robust early marker of functional response to exercise, the investigators will have an easy-to-deploy predictor of who will best benefit from HIIT. In aim 2 the investigators will determine if (a) baseline GABA and/or CBF predict improvements in walking speed from baseline to after HIIT and (b) if a change in GABA and/or CBF relate to a change in walking speed. The investigators aim to establish neurophysiological correlates of improving function with HIIT to better understand the mechanisms. Finally, in aim 3 the investigators will a predictive machine learning algorithm of who will improve their walking speed with HIIT using factors of blood lactate, baseline GABA and CBF, baseline leg weakness and VO2-max, pre-stroke fitness, age, sex, and comorbidities. The overarching objective is to develop a model to predict which Veteran with chronic stroke will respond to a 12-week exercise program.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • chronic left or right subcortical stroke as defined by 6 months or more after a cardiovascular accident
  • lower extremity motor impairment due to stroke that causes a walking speed of less than 0.6 m/s during a 10m walk
  • Veteran status

Exclusion criteria

  • MRI contraindications, including implanted cardiac pacemakers and severe claustrophobia
  • any neurodegenerative condition other than stroke that may lead to lower extremity impairment
  • a visual or auditory impairment that may hinder study procedures
  • any medical condition that would preclude participation in a physical exercise intervention program

Treatment and study plan

High Intensity Interval Training (HIIT)

Other

HIIT consists of three weekly 25-60 minute cycling sessions for 12 weeks at the Atlanta VA, administered by a trained exercise physiologist, for a total of 36 HIIT sessions.

Primary outcomes

  1. 10 m walk test on a GAITRite mat

    Time frame: baseline (week 1) and after the completion of 12 weeks of exercise (week 14)

    To assess short-distance walking speed and gait characteristics.

  2. Timed-Up-and-Go (TUG) test

    Time frame: baseline (week 1) and after the completion of 12 weeks of exercise (week 14)

    To assess short-distance walking and postural control.

  3. 6-minute walk test

    Time frame: baseline (week 1) and after the completion of 12 weeks of exercise (week 14)

    To assess endurance.

Secondary outcomes

  1. Blood lactate change during HIIT session

    Time frame: On exercise day 1, 4, 7, 10, and 28. The total number of exercise days is 36 (3 times per week for 12 weeks).

    To assess if the participant increases their blood lactate during the HIIT session.

  2. MEGA-PRESS Magnetic Resonance Spectroscopy

    Time frame: baseline (week 1) and after the completion of 12 weeks of exercise (week 14)

    To assess GABA from the ipsilesional and contralesional leg areas of the brain.

  3. pseudo Continuous Arterial Spin Labeling MRI

    Time frame: baseline (week 1) and after the completion of 12 weeks of exercise (week 14)

    To assess whole brain regional cerebral blood flow.

  4. Graded treadmill or bike testing

    Time frame: baseline (week 1) and after the completion of 12 weeks of exercise (week 14)

    To estimate VO2-max.

Other outcomes

  1. Repetition max strength test

    Time frame: baseline (week 1) and after the completion of 12 weeks of exercise (week 14)

    To assess the leg strength of the affected and less affected leg.

  2. Global physical activity questionnaire (GPAQ)

    Time frame: baseline (week 1)

    To assess pre-stroke fitness levels.

  3. Self-administered Comorbidity Questionnaire (SCQ)

    Time frame: baseline (week 1) and after the completion of 12 weeks of exercise (week 14)

    To assess the presence and burden of comorbidities.

Study contacts

Contact information is provided by the study sponsor or research team.

Lisa C Krishnamurthy, PhD

CONTACT

[email protected]

(404) 321-6111 ext. 6235

Sponsors and collaborators

Lead sponsor

VA Office of Research and Development

Fed

Collaborators

  • Atlanta VA Medical Center

Registry information

Official study title

What Makes a Responder, a Responder? Biomarkers to Help Identify Responders and Resistors to High-intensity Interval Training for Lower Extremity Chronic Stroke

Acronym: BReaTHE

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Sep 29, 2023
Registry last updated
Mar 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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